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Plan now to ensure your medical devices comply with new IEC 60601-1-2 EMC 4th Edition standard requirements by the December 2018 effective date. Since the development cycle can be 2-3 years, it is important to understand the new standard now when designing medical devices.
To provide you guidance on these important changes and improve your speed to market, Intertek's industry experts developed this complimentary white paper. The paper features detailed information on the Risk Management File, test planning, emissions and immunity testing requirements as well as a roadmap for expected implementation in markets throughout the world.